AP2324A - Polymorphic forms of 3-(4-amino-1-oxo-1,3 dihydro-isoindol-2-yl)-piperidine-2,6-dione. - Google Patents

Polymorphic forms of 3-(4-amino-1-oxo-1,3 dihydro-isoindol-2-yl)-piperidine-2,6-dione.

Info

Publication number
AP2324A
AP2324A AP2006003558A AP2006003558A AP2324A AP 2324 A AP2324 A AP 2324A AP 2006003558 A AP2006003558 A AP 2006003558A AP 2006003558 A AP2006003558 A AP 2006003558A AP 2324 A AP2324 A AP 2324A
Authority
AP
ARIPO
Prior art keywords
isoindol
dione
piperidine
dihydro
oxo
Prior art date
Application number
AP2006003558A
Other versions
AP2006003558A0 (en
Inventor
Roger Chen
George W Muller
Markian S Jaworsky
Original Assignee
Celgene Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=34272860&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AP2324(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Celgene Corp filed Critical Celgene Corp
Publication of AP2006003558A0 publication Critical patent/AP2006003558A0/en
Application granted granted Critical
Publication of AP2324A publication Critical patent/AP2324A/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D51/00Closures not otherwise provided for
    • B65D51/24Closures not otherwise provided for combined or co-operating with auxiliary devices for non-closing purposes
    • B65D51/28Closures not otherwise provided for combined or co-operating with auxiliary devices for non-closing purposes with auxiliary containers for additional articles or materials
    • B65D51/2807Closures not otherwise provided for combined or co-operating with auxiliary devices for non-closing purposes with auxiliary containers for additional articles or materials the closure presenting means for placing the additional articles or materials in contact with the main contents by acting on a part of the closure without removing the closure, e.g. by pushing down, pulling up, rotating or turning a part of the closure, or upon initial opening of the container
    • B65D51/2857Closures not otherwise provided for combined or co-operating with auxiliary devices for non-closing purposes with auxiliary containers for additional articles or materials the closure presenting means for placing the additional articles or materials in contact with the main contents by acting on a part of the closure without removing the closure, e.g. by pushing down, pulling up, rotating or turning a part of the closure, or upon initial opening of the container the additional article or materials being released by displacing or removing an element enclosing it
    • B65D51/2864Closures not otherwise provided for combined or co-operating with auxiliary devices for non-closing purposes with auxiliary containers for additional articles or materials the closure presenting means for placing the additional articles or materials in contact with the main contents by acting on a part of the closure without removing the closure, e.g. by pushing down, pulling up, rotating or turning a part of the closure, or upon initial opening of the container the additional article or materials being released by displacing or removing an element enclosing it the element being a plug or like element closing a passage between the auxiliary container and the main container
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Pain & Pain Management (AREA)
  • Epidemiology (AREA)
  • Hematology (AREA)
  • Mechanical Engineering (AREA)
  • Diabetes (AREA)
  • Oncology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Rheumatology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Transplantation (AREA)
  • Cardiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Medicinal Preparation (AREA)
  • Indole Compounds (AREA)
AP2006003558A 2003-09-04 2004-09-03 Polymorphic forms of 3-(4-amino-1-oxo-1,3 dihydro-isoindol-2-yl)-piperidine-2,6-dione. AP2324A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US49972303P 2003-09-04 2003-09-04
PCT/US2004/028736 WO2005023192A2 (en) 2003-09-04 2004-09-03 Polymorphic forms of 3-(4-amino-1-oxo-1,3 dihydro-isoindol-2-yl)-piperidine-2,6-dione

Publications (2)

Publication Number Publication Date
AP2006003558A0 AP2006003558A0 (en) 2006-04-30
AP2324A true AP2324A (en) 2011-11-21

Family

ID=34272860

Family Applications (1)

Application Number Title Priority Date Filing Date
AP2006003558A AP2324A (en) 2003-09-04 2004-09-03 Polymorphic forms of 3-(4-amino-1-oxo-1,3 dihydro-isoindol-2-yl)-piperidine-2,6-dione.

Country Status (37)

Country Link
US (20) US7465800B2 (en)
EP (7) EP2425836A1 (en)
JP (6) JP4733037B2 (en)
KR (3) KR20080063862A (en)
CN (7) CN101863878B (en)
AP (1) AP2324A (en)
AR (2) AR047994A1 (en)
AT (1) ATE531369T1 (en)
AU (2) AU2004270211B2 (en)
BR (1) BRPI0414084A (en)
CA (9) CA2741575C (en)
CR (2) CR8291A (en)
CY (1) CY1112017T1 (en)
DK (5) DK3045176T3 (en)
EA (1) EA009922B1 (en)
EC (1) ECSP066467A (en)
ES (5) ES2402808T3 (en)
GE (1) GEP20104958B (en)
HK (1) HK1202531A1 (en)
HR (1) HRP20110836T1 (en)
HU (3) HUE041282T2 (en)
IL (5) IL174067A (en)
IS (1) IS8340A (en)
MA (1) MA28084A1 (en)
ME (3) ME01530B (en)
MX (6) MX346372B (en)
NO (4) NO336898B1 (en)
NZ (1) NZ546054A (en)
OA (1) OA13250A (en)
PE (1) PE20060284A1 (en)
PL (5) PL3042659T3 (en)
PT (5) PT1667682E (en)
RS (3) RS20060158A (en)
SI (2) SI1667682T1 (en)
UA (1) UA83504C2 (en)
WO (1) WO2005023192A2 (en)
ZA (1) ZA200601858B (en)

Families Citing this family (108)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HU228769B1 (en) * 1996-07-24 2013-05-28 Celgene Corp Substituted 2(2,6-dioxopiperidin-3-yl)phthalimides and -1-oxoisoindolines and their use for production of pharmaceutical compositions for mammals to reduce the level of tnf-alpha
US7629360B2 (en) * 1999-05-07 2009-12-08 Celgene Corporation Methods for the treatment of cachexia and graft v. host disease
US6458810B1 (en) 2000-11-14 2002-10-01 George Muller Pharmaceutically active isoindoline derivatives
MXPA03004699A (en) * 2000-11-30 2005-01-25 Childrens Medical Center Synthesis of 3-amino-thalidomide and its enantiomers.
US7323479B2 (en) * 2002-05-17 2008-01-29 Celgene Corporation Methods for treatment and management of brain cancer using 1-oxo-2-(2,6-dioxopiperidin-3-yl)-4-methylisoindoline
US7968569B2 (en) 2002-05-17 2011-06-28 Celgene Corporation Methods for treatment of multiple myeloma using 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione
USRE48890E1 (en) 2002-05-17 2022-01-11 Celgene Corporation Methods for treating multiple myeloma with 3-(4-amino-1-oxo-1,3-dihydroisoindol-2-yl)-piperidine-2,6-dione after stem cell transplantation
US8404716B2 (en) 2002-10-15 2013-03-26 Celgene Corporation Methods of treating myelodysplastic syndromes with a combination therapy using lenalidomide and azacitidine
US11116782B2 (en) 2002-10-15 2021-09-14 Celgene Corporation Methods of treating myelodysplastic syndromes with a combination therapy using lenalidomide and azacitidine
UA83504C2 (en) 2003-09-04 2008-07-25 Селджин Корпорейшн Polymorphic forms of 3-(4-amino-1-oxo-1,3 dihydro-isoindol-2-yl)-piperidine-2,6-dione
US20050143344A1 (en) * 2003-12-30 2005-06-30 Zeldis Jerome B. Methods and compositions using immunomodulatory compounds for the treatment and management of central nervous system disorders or diseases
US20050222209A1 (en) * 2004-04-01 2005-10-06 Zeldis Jerome B Methods and compositions for the treatment, prevention or management of dysfunctional sleep and dysfunctional sleep associated with disease
BRPI0510110A (en) * 2004-04-23 2007-09-25 Celgene Corp method for treating, preventing or controlling pulmonary hypertension, and pharmaceutical composition
WO2007005807A2 (en) * 2005-06-30 2007-01-11 Anthrogenesis Corporation Repair of tympanic membrane using placenta derived collagen biofabric
RS52704B (en) 2005-06-30 2013-08-30 Celgene Corporation Processes for the preparation of 4-amino-2-(2,6-dioxopiperidin-3-yl) isoindoline-1,3-dione compounds
WO2007009062A2 (en) * 2005-07-13 2007-01-18 Anthrogenesis Corporation Treatment of leg ulcers using placenta derived collagen biofabric
US20070021762A1 (en) * 2005-07-13 2007-01-25 Qing Liu Ocular plug formed from placenta derived collagen biofabric
US20070066512A1 (en) * 2005-09-12 2007-03-22 Dominique Verhelle Methods and compositions using immunomodulatory compounds for the treatment of disorders associated with low plasma leptin levels
WO2007136640A2 (en) * 2006-05-16 2007-11-29 Celgene Corporation Processes for the preparation of substituted 2-(2,6-dioxopiperidin-3-yl)isoindole-1,3-dione
US8105634B2 (en) * 2006-08-15 2012-01-31 Anthrogenesis Corporation Umbilical cord biomaterial for medical use
WO2008042441A1 (en) * 2006-10-03 2008-04-10 Anthrogenesis Corporation Use of umbilical cord biomaterial for ocular surgery
WO2008060377A2 (en) 2006-10-04 2008-05-22 Anthrogenesis Corporation Placental or umbilical cord tissue compositions
KR20190112868A (en) 2006-10-06 2019-10-07 안트로제네시스 코포레이션 Native(telopeptide) Placental Collagen Compositions
PT2203176E (en) 2007-09-28 2015-03-02 Anthrogenesis Corp TUMOR SUPPRESSION USING HUMAN PLACENTARY PERFUSION AND INTERMEDIATE NATURAL MURDER CELLS DERIVED FROM HUMAN PLACENTA
US7964354B2 (en) * 2007-12-20 2011-06-21 Celgene Corporation Use of micro-RNA as a biomarker of immunomodulatory drug activity
JP2011513497A (en) * 2008-03-11 2011-04-28 ドクター・レディーズ・ラボラトリーズ・リミテッド Preparation of lenalidomide
US20110060010A1 (en) * 2008-03-13 2011-03-10 Tianjin Hemay Bio-Tech Co., Ltd Salts of 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)piperidine-2,6-dione and derivatives thereof, or polymorphs of salts, process for preparing same and use thereof
AU2009321374A1 (en) * 2008-11-03 2010-06-03 Generics [Uk] Limited A crystalline form of lenalidomide and a process for its preparation
DE102008057335A1 (en) 2008-11-14 2010-05-20 Ratiopharm Gmbh Intermediate, useful e.g. as an immunomodulator, for inhibiting the proliferation of certain hematopoietic tumor cells and stimulating erythropoiesis, comprises amorphous lenalidomide and a surface stabilizer
DE102008057285A1 (en) 2008-11-14 2010-05-20 Ratiopharm Gmbh New intermediate comprising lenalidomide and matrix material, in the form of a solid solution, useful e.g. as immunomodulatory drug, to inhibit proliferation of hematopoietic tumor cells and promote T-cell and natural killer cell immunity
DE102008057284A1 (en) 2008-11-14 2010-05-20 Ratiopharm Gmbh Preparation of tablets containing lenalidomide and adhesion promoter, where the tablets are produced by dry granulation or direct compression, useful e.g. for stimulating erythropoiesis and as an immunomodulator
WO2010054833A1 (en) * 2008-11-14 2010-05-20 Ratiopharm Gmbh Intermediate and oral administrative formats containing lenalidomide
AU2009314512B2 (en) * 2008-11-17 2013-04-04 Dr. Reddy's Laboratories Ltd. Lenalidomide solvates and processes
EP2367553B1 (en) 2008-12-05 2017-05-03 Novo Nordisk A/S Combination therapy to enhance nk cell mediated cytotoxicity
DK2403845T3 (en) 2009-03-02 2014-08-04 Generics Uk Ltd Improved process.
WO2010129636A2 (en) * 2009-05-08 2010-11-11 Dr. Reddy's Laboratories Ltd. Lenalidomide polymorph
MX342330B (en) 2009-05-19 2016-09-26 Celgene Corp Formulations of 4-amino-2-(2,6-dioxopiperidine-3-yl)isoindoline-1 ,3-dione.
CN101665484B (en) * 2009-07-20 2012-11-21 上海皓元生物医药科技有限公司 Method for preparing lenalidomide
EP2464638A1 (en) 2009-08-12 2012-06-20 Synthon B.V. Lenalidomide salts
WO2011033468A1 (en) 2009-09-16 2011-03-24 Ranbaxy Laboratories Limited Process for the preparation of a crystalline form of lenalidomid
TWI475014B (en) * 2009-09-17 2015-03-01 Scinopharm Taiwan Ltd Solid forms of 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2, 6-dione and methods of making the same
WO2011050962A1 (en) 2009-10-29 2011-05-05 Ratiopharm Gmbh Acid addition salts of lenalidomide
CN102060842B (en) * 2009-11-02 2013-05-08 南京卡文迪许生物工程技术有限公司 3-(substituted xylylenimine-2-yl)-2,6-piperidine diketone polymorph and medical composition
CN101696205B (en) 2009-11-02 2011-10-19 南京卡文迪许生物工程技术有限公司 3-(Substituted dihydroisoindol-2-yl)-2,6-piperidinedione polymorph and pharmaceutical composition
CN102127054B (en) * 2009-11-02 2013-04-03 南京卡文迪许生物工程技术有限公司 3-(substituted dihydroisoindol-2-yl)-2,6-piperidinedione polymorph and pharmaceutical composite
WO2011061611A1 (en) 2009-11-19 2011-05-26 Ranbaxy Laboratories Limited Process for the preparation of form b of lenalidomide
WO2011069608A1 (en) 2009-12-09 2011-06-16 Ratiopharm Gmbh S-lenalidomide, polymorphic forms thereof and blend comprising s- und r-lenalidomide
CN101817813B (en) * 2010-01-15 2013-04-10 南京卡文迪许生物工程技术有限公司 Crystal IV of 3-(substituted dihydroisoindolinone-2-yl)-2,6-piperidinediketone and medicinal composite thereof
UA114856C2 (en) 2010-02-11 2017-08-10 Селджин Корпорейшн METHODS OF TREATMENT WITH THE APPLICATION OF ARYLMETOXISOINDOLINE DERIVATIVES
CA2793312C (en) 2010-03-08 2016-06-14 Natco Pharma Limited Anhydrous lenalidomide form-i
EP2582836B1 (en) 2010-06-18 2018-03-07 Taiho Pharmaceutical Co., Ltd. Prpk-tprkb modulators and uses thereof
US9918197B2 (en) 2010-10-04 2018-03-13 Lazo Inc. Interactive advertisement environment
US20140031325A1 (en) 2010-12-06 2014-01-30 Celgene Corporation Combination therapy with lenalidomide and a cdk inhibitor for treating multiple myeloma
CN102070606A (en) * 2011-02-17 2011-05-25 江苏先声药物研究有限公司 New method for preparing LenalidomideA crystal form
CN102643266B (en) * 2011-02-17 2015-02-18 江苏先声药物研究有限公司 New preparation method of Lenalidomide B crystal form
TWI540127B (en) 2011-03-11 2016-07-01 西建公司 Solid form of 3-(5-amino-2-methyl-4-oxy-4H-quinazolin-3-yl)-hexahydropyridine-2,6-dione, and pharmaceutical composition and use thereof
EP2688649B1 (en) * 2011-03-23 2019-04-10 Hetero Research Foundation A polymorph of lenalidomide
AU2012236655B2 (en) 2011-03-28 2016-09-22 Deuterx, Llc, 2',6'-dioxo-3'-deutero-piperdin-3-yl-isoindoline compounds
WO2013005229A1 (en) * 2011-07-05 2013-01-10 Hetero Research Foundation Process for lenalidomide
US9643950B2 (en) * 2012-10-22 2017-05-09 Concert Pharmaceuticals, Inc. Solid forms of {s-3-(4-amino-1-oxo-isoindolin-2-yl)(piperidine-3,4,4,5,5-d5)-2,6-dione}
WO2014110322A2 (en) 2013-01-11 2014-07-17 Concert Pharmaceuticals, Inc. Substituted dioxopiperidinyl phthalimide derivatives
EP2943201B2 (en) 2013-01-14 2020-07-29 Deuterx, LLC 3-(5-substituted-4-oxoquinazolin-3(4h)-yl)-3-deutero-piperidine-2,6-dione derivatives
CN115282165A (en) 2013-02-05 2022-11-04 细胞结构公司 Natural killer cells from placenta
US9290475B2 (en) 2013-03-14 2016-03-22 Deuterx, Llc 3-(substituted-4-oxoquinazolin-3(4H)-yl)-3-deutero-piperidine-2,6-dione derivatives and compositions comprising and methods of using the same
CN104072476B (en) * 2013-03-27 2018-08-21 江苏豪森药业集团有限公司 Pomalidomide crystal and its preparation method and application
EP2981532A4 (en) * 2013-04-01 2016-12-14 Hetero Research Foundation Process for pomalidomide
WO2015034871A2 (en) * 2013-09-03 2015-03-12 Fugro Chance, Inc. Interactive remote guidance system for seaborne vessels
UA117141C2 (en) 2013-10-08 2018-06-25 Селджин Корпорейшн COMPOSITIONS (S) -3- (4 - ((4- (MORPHOLINOMETHYL) BENZYL) OXY) -1-OXOISOINDOLIN-2-IL) PIPERIDINE-2,6-DIONE
EP2875817B1 (en) * 2013-11-26 2020-03-18 Synhton B.V. Pharmaceutical formulation comprising amorphous lenalidomide
AU2015210999A1 (en) 2014-01-29 2016-07-21 Otsuka Pharmaceutical Co., Ltd. Device-based risk management of a therapeutic
WO2015113314A1 (en) * 2014-01-30 2015-08-06 上海创诺制药有限公司 New crystal form of 3-(4-amino-1,3-dihydro-1-oxo-2h-isoindole-2-yl)-2,6-piperidinedione and preparation method therefor
CN104016966A (en) * 2014-01-30 2014-09-03 上海创诺制药有限公司 Novel 3-(4-amino-1,3-dihydro-1-oxo-2H-isoindole-2-yl)-2,6-piperidinedione crystal forms and preparation method thereof
SG10201809280PA (en) * 2014-04-22 2018-11-29 Otsuka Pharma Co Ltd Combination of brexpiprazole and nalmefene and use thereof for treating substance-related disorders
CN105085473B (en) * 2014-04-24 2019-06-18 江苏豪森药业集团有限公司 Lenalidomide crystal form and preparation method thereof and medical usage
EP3137450A2 (en) * 2014-04-26 2017-03-08 Shilpa Medicare Limited Crystalline lenalidomide process
US20150348512A1 (en) * 2014-06-01 2015-12-03 Apple Inc. Method and apparatus for representing a device's traversal along a route
US10392364B2 (en) 2014-08-11 2019-08-27 Avra Laboratories Pvt. Ltd. Process for synthesis of lenalidomide
SMT202300081T1 (en) 2014-08-22 2023-05-12 Celgene Corp Methods of treating multiple myeloma with immunomodulatory compounds in combination with antibodies
US9794331B1 (en) * 2014-09-29 2017-10-17 Amazon Technologies, Inc. Block allocation based on server utilization
EP3233082B1 (en) 2014-12-19 2018-12-05 Synthon B.V. Pharmaceutical composition comprising amorphous lenalidomide
US10507204B2 (en) 2014-12-19 2019-12-17 Synthon B.V. Pharmaceutical composition comprising amorphous lenalidomide
CN104447689B (en) * 2014-12-22 2016-07-20 上海迈柏医药科技有限公司 Crystal formation of lenalidomide and preparation method thereof
CN104610210B (en) * 2015-02-05 2017-06-16 天津大学 A kind of sodium dehydroacetate anhydride preparation method
US9809603B1 (en) 2015-08-18 2017-11-07 Deuterx, Llc Deuterium-enriched isoindolinonyl-piperidinonyl conjugates and oxoquinazolin-3(4H)-yl-piperidinonyl conjugates and methods of treating medical disorders using same
ES2811110T3 (en) 2015-08-27 2021-03-10 Grindeks Jsc Pharmaceutical composition capable of incorporating Lenalidomide in various crystalline modifications
EA036205B1 (en) 2015-12-22 2020-10-14 Синтон Б.В. Pharmaceutical composition comprising amorphous lenalidomide and an antioxidant
RU2616976C1 (en) * 2016-04-07 2017-04-19 Олег Ростиславович Михайлов CRYSTALLINE β-MODIFICATION OF 3-(4-AMINO-1-OXO-1,3-DIHYDRO-2H-ISOINDOL-2-YL)-PIPERIDINE-2,6-DIONE, METHOD OF ITS PRODUCTION AND PHARMACEUTICAL COMPOSITION BASED THEREON
WO2018013693A1 (en) 2016-07-13 2018-01-18 Celgene Corporation Solid dispersions and cocrystals comprising 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione compositions and methods of use thereof
TWI664172B (en) * 2016-08-25 2019-07-01 大陸商浙江海正藥業股份有限公司 Crystal form of lenalidomide, preparation method and application thereof
US11584733B2 (en) 2017-01-09 2023-02-21 Shuttle Pharmaceuticals, Inc. Selective histone deacetylase inhibitors for the treatment of human disease
CA3049435A1 (en) 2017-01-09 2018-07-12 Scott Grindrod Selective histone deacetylase inhibitors for the treatment of human disease
CN108658935A (en) * 2017-03-27 2018-10-16 天津大学 Lenalidomide novel crystal forms, preparation method and its medical usage
US10093647B1 (en) 2017-05-26 2018-10-09 Celgene Corporation Crystalline 4-amino-2-(2,6-dioxopiperidine-3-yl)isoindoline-1,3-dione dihydrate, compositions and methods of use thereof
CN107400115A (en) * 2017-08-04 2017-11-28 正大天晴药业集团股份有限公司 A new crystal of lenalidomide and its pharmaceutical composition
BR112020005077A2 (en) 2017-09-14 2020-09-15 Glaxosmithkline Intellectual Property Development Limited combination treatment for cancer
US10093648B1 (en) 2017-09-22 2018-10-09 Celgene Corporation Crystalline 4-amino-2-(2,6-dioxopiperidine-3-yl)isoindoline-1,3-dione hemihydrate, compositions and methods of use thereof
US10093649B1 (en) 2017-09-22 2018-10-09 Celgene Corporation Crystalline 4-amino-2-(2,6-dioxopiperidine-3-yl)isoindoline-1,3-dione monohydrate, compositions and methods of use thereof
WO2019067792A1 (en) 2017-09-28 2019-04-04 Celularity, Inc. Tumor suppression using human placenta-derived intermediate natural killer (pink) cells in combination with an antibody
RU2020110236A (en) 2017-10-26 2021-11-26 Синбиас Фарма АГ IMMEDIATE RELEASE LENALIDOMIDE COMPOSITION
EP3505158A1 (en) 2017-12-27 2019-07-03 KRKA, d.d., Novo mesto Pharmaceutical composition of lenalidomide pharmaceutically acceptable acid addition salt
CN108191826A (en) * 2018-01-08 2018-06-22 浙江省医学科学院 A kind of lenalidomide crystal and preparation method thereof
US11407723B2 (en) 2018-01-09 2022-08-09 Shuttle Pharmaceuticals, Inc. Selective histone deacetylase inhibitors for the treatment of human disease
WO2019138424A1 (en) 2018-01-11 2019-07-18 Natco Pharma Limited Stable pharmaceutical compositions comprising lenalidomide
CN108840908A (en) * 2018-07-10 2018-11-20 刘凤娟 A kind of novel crystal forms of telavi and preparation method thereof
CN111217792B (en) * 2018-11-23 2021-09-28 欣凯医药化工中间体(上海)有限公司 Preparation method of lenalidomide B crystal form
JP2024503001A (en) 2021-01-08 2024-01-24 スタートン セラピューティクス インコーポレイテッド Stable solutions of immunomodulatory imide compounds for parenteral use
EP4456876A1 (en) 2021-12-31 2024-11-06 a Fine House S.A. Lenalidomide oral solution
EP4456875B1 (en) 2021-12-31 2025-10-15 a Fine House S.A. Oral solution comprising lenalidomide

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6316471B1 (en) * 1996-07-24 2001-11-13 Celgene Corporation Isoindolines, method of use, and pharmaceutical compositions

Family Cites Families (95)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3536809A (en) 1969-02-17 1970-10-27 Alza Corp Medication method
US3598123A (en) 1969-04-01 1971-08-10 Alza Corp Bandage for administering drugs
US3845770A (en) 1972-06-05 1974-11-05 Alza Corp Osmatic dispensing device for releasing beneficial agent
US3916899A (en) 1973-04-25 1975-11-04 Alza Corp Osmotic dispensing device with maximum and minimum sizes for the passageway
US4008719A (en) 1976-02-02 1977-02-22 Alza Corporation Osmotic system having laminar arrangement for programming delivery of active agent
IE58110B1 (en) 1984-10-30 1993-07-14 Elan Corp Plc Controlled release powder and process for its preparation
US5391485A (en) 1985-08-06 1995-02-21 Immunex Corporation DNAs encoding analog GM-CSF molecules displaying resistance to proteases which cleave at adjacent dibasic residues
US4810643A (en) 1985-08-23 1989-03-07 Kirin- Amgen Inc. Production of pluripotent granulocyte colony-stimulating factor
JPS63500636A (en) 1985-08-23 1988-03-10 麒麟麦酒株式会社 DNA encoding multipotent granulocyte colony stimulating factor
US5073543A (en) 1988-07-21 1991-12-17 G. D. Searle & Co. Controlled release formulations of trophic factors in ganglioside-lipsome vehicle
IT1229203B (en) 1989-03-22 1991-07-25 Bioresearch Spa USE OF 5 METHYLTHETRAHYDROPHOLIC ACID, 5 FORMYLTHETRAHYDROPHOLIC ACID AND THEIR PHARMACEUTICALLY ACCEPTABLE SALTS FOR THE PREPARATION OF PHARMACEUTICAL COMPOSITIONS IN THE FORM OF CONTROLLED RELEASE ACTIVE IN THE THERAPY OF MENTAL AND ORGANIC DISORDERS.
US5120548A (en) 1989-11-07 1992-06-09 Merck & Co., Inc. Swelling modulated polymeric drug delivery device
US5733566A (en) 1990-05-15 1998-03-31 Alkermes Controlled Therapeutics Inc. Ii Controlled release of antiparasitic agents in animals
AU1531492A (en) 1991-02-14 1992-09-15 Rockefeller University, The Method for controlling abnormal concentration tnf alpha in human tissues
US5580578A (en) 1992-01-27 1996-12-03 Euro-Celtique, S.A. Controlled release formulations coated with aqueous dispersions of acrylic polymers
US5360352A (en) 1992-12-24 1994-11-01 The Whitaker Corporation Wire retainer for current mode coupler
US5591767A (en) 1993-01-25 1997-01-07 Pharmetrix Corporation Liquid reservoir transdermal patch for the administration of ketorolac
US6228879B1 (en) 1997-10-16 2001-05-08 The Children's Medical Center Methods and compositions for inhibition of angiogenesis
US20010056114A1 (en) 2000-11-01 2001-12-27 D'amato Robert Methods for the inhibition of angiogenesis with 3-amino thalidomide
US5629327A (en) 1993-03-01 1997-05-13 Childrens Hospital Medical Center Corp. Methods and compositions for inhibition of angiogenesis
US6114355A (en) 1993-03-01 2000-09-05 D'amato; Robert Methods and compositions for inhibition of angiogenesis
US5698579A (en) * 1993-07-02 1997-12-16 Celgene Corporation Cyclic amides
IT1270594B (en) 1994-07-07 1997-05-07 Recordati Chem Pharm CONTROLLED RELEASE PHARMACEUTICAL COMPOSITION OF LIQUID SUSPENSION MOGUISTEIN
ATE205723T1 (en) * 1994-11-04 2001-10-15 Polymun Scient Immunbio Forsch APPLICATION OF SOD IN LIPOSOMES
US5731325A (en) 1995-06-06 1998-03-24 Andrulis Pharmaceuticals Corp. Treatment of melanomas with thalidomide alone or in combination with other anti-melanoma agents
DE19601303A1 (en) 1996-01-16 1997-07-17 Boehringer Ingelheim Kg Novel benzoylguanidine derivatives, process for their preparation and their use in the manufacture of medicaments
WO1997046526A1 (en) 1996-06-07 1997-12-11 Eisai Co., Ltd. Stable polymorphs of donepezil (1-benzyl-4-[(5,6-dimethoxy-1-indanon)-2-yl]methylpiperidine) hydrochloride and process for production
JPH1053576A (en) * 1996-06-07 1998-02-24 Eisai Co Ltd Polymorphic crystal of donepezil hydrochloride and its production
JP4065567B2 (en) 1996-07-24 2008-03-26 セルジーン コーポレイション Substituted 2- (2,6-dioxopiperidin-3-yl) phthalimides and -1-oxoisoindolines and methods for reducing TNFα levels
US5798368A (en) * 1996-08-22 1998-08-25 Celgene Corporation Tetrasubstituted 2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolines and method of reducing TNFα levels
HU228769B1 (en) * 1996-07-24 2013-05-28 Celgene Corp Substituted 2(2,6-dioxopiperidin-3-yl)phthalimides and -1-oxoisoindolines and their use for production of pharmaceutical compositions for mammals to reduce the level of tnf-alpha
US5635517B1 (en) 1996-07-24 1999-06-29 Celgene Corp Method of reducing TNFalpha levels with amino substituted 2-(2,6-dioxopiperidin-3-YL)-1-oxo-and 1,3-dioxoisoindolines
SK17799A3 (en) * 1996-08-12 1999-11-08 Celgene Corp Cyano and carboxy derivatives of substituted styrenes, pharmaceutical composition containing same and their use
DK0963200T3 (en) 1996-11-05 2005-10-24 Childrens Medical Center Preparations for inhibiting angiogenesis comprising thalidomide and an NSAID
WO1998035021A1 (en) 1997-02-05 1998-08-13 University Of Hertfordshire Preparation of spheroids and their use in medicin or diagnosis
US5874448A (en) * 1997-11-18 1999-02-23 Celgene Corporation Substituted 2-(2,6 dioxo-3-fluoropiperidin-3-yl)-isoindolines and method of reducing TNFα levels
US5955476A (en) * 1997-11-18 1999-09-21 Celgene Corporation Substituted 2-(2,6-dioxo-3-fluoropiperidin-3-yl)-isoindolines and method of reducing inflammatory cytokine levels
KR20070040423A (en) 1998-03-16 2007-04-16 셀진 코포레이션 2- (2,6-dioxopiperidin-3-yl) isoindolin derivatives for inflammatory cytokine inhibitors, preparations thereof and uses thereof
US6673828B1 (en) * 1998-05-11 2004-01-06 Children's Medical Center Corporation Analogs of 2-Phthalimidinoglutaric acid
US6020358A (en) 1998-10-30 2000-02-01 Celgene Corporation Substituted phenethylsulfones and method of reducing TNFα levels
US20030013739A1 (en) 1998-12-23 2003-01-16 Pharmacia Corporation Methods of using a combination of cyclooxygenase-2 selective inhibitors and thalidomide for the treatment of neoplasia
RU2001121987A (en) * 1999-03-18 2004-02-27 Селджин Корпорейшн (Us) Substituted 1-oxo- and 1,3-dioxoisoindolines and their use in pharmaceutical compositions to reduce inflammatory cytokines
US7182953B2 (en) 1999-12-15 2007-02-27 Celgene Corporation Methods and compositions for the prevention and treatment of atherosclerosis restenosis and related disorders
US6326388B1 (en) 1999-12-21 2001-12-04 Celgene Corporation Substituted 1,3,4-oxadiazoles and a method of reducing TNF-alpha level
KR20020071931A (en) * 2000-01-07 2002-09-13 트렌스폼 파마수티컬스 인코퍼레이티드 High-throughput formation, identification, and analysis of diverse solid-forms
CA2319872C (en) 2000-02-02 2012-06-19 Chun-Ying Huang Pharmaceutical composition for the treatment of hepatocellular carcinoma
HUP0204562A2 (en) 2000-03-17 2003-04-28 Cell Therapeutics, Inc. Polyglutamic acid-camptothecin conjugates and methods of preparation and pharmaceutical compositions containing the same
JP2003528918A (en) 2000-03-31 2003-09-30 セルジーン コーポレイション Inhibition of cyclooxygenase-2 activity
DK1307197T3 (en) 2000-05-15 2006-07-03 Celgene Corp Compositions for the treatment of cancer containing a topoisomerase inhibitor and thalidomide
HUP0301161A3 (en) * 2000-09-26 2005-04-28 Reddy S Res Foundation Hyderab Novel polymorphic forms of 5-[4-[2-[n-methyl-n-(2-pyridyl)amino]ethoxy]benzyl]thiazolidine-2,4-dione maleate and process for their preparation
US6458810B1 (en) 2000-11-14 2002-10-01 George Muller Pharmaceutically active isoindoline derivatives
MXPA03004699A (en) 2000-11-30 2005-01-25 Childrens Medical Center Synthesis of 3-amino-thalidomide and its enantiomers.
US20020128228A1 (en) 2000-12-01 2002-09-12 Wen-Jen Hwu Compositions and methods for the treatment of cancer
US7091353B2 (en) * 2000-12-27 2006-08-15 Celgene Corporation Isoindole-imide compounds, compositions, and uses thereof
US20030045552A1 (en) 2000-12-27 2003-03-06 Robarge Michael J. Isoindole-imide compounds, compositions, and uses thereof
JP4361273B2 (en) 2001-02-27 2009-11-11 アメリカ合衆国 Thalidomide analogs as potential angiogenesis inhibitors
EP1423115B9 (en) 2001-08-06 2009-09-02 The Children's Medical Center Corporation Antiangiogenic activity of nitrogen substituted thalidomide analogs
US6472563B1 (en) 2001-11-09 2002-10-29 Sepracor Inc. Formoterol tartrate process and polymorph
KR20050000398A (en) 2002-04-12 2005-01-03 셀진 코포레이션 Methods for identification of modulators of angiogenesis, compounds discovered thereby, and methods of treatment using the compounds
US7498171B2 (en) 2002-04-12 2009-03-03 Anthrogenesis Corporation Modulation of stem and progenitor cell differentiation, assays, and uses thereof
ES2521672T3 (en) 2002-05-17 2014-11-13 Celgene Corporation Pharmaceutical formulations for cancer treatment
US7968569B2 (en) * 2002-05-17 2011-06-28 Celgene Corporation Methods for treatment of multiple myeloma using 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione
US7323479B2 (en) 2002-05-17 2008-01-29 Celgene Corporation Methods for treatment and management of brain cancer using 1-oxo-2-(2,6-dioxopiperidin-3-yl)-4-methylisoindoline
US7189740B2 (en) * 2002-10-15 2007-03-13 Celgene Corporation Methods of using 3-(4-amino-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione for the treatment and management of myelodysplastic syndromes
US20050203142A1 (en) * 2002-10-24 2005-09-15 Zeldis Jerome B. Methods of using and compositions comprising immunomodulatory compounds for treatment, modification and management of pain
US20040091455A1 (en) * 2002-10-31 2004-05-13 Zeldis Jerome B. Methods of using and compositions comprising immunomodulatory compounds for treatment and management of macular degeneration
US7563810B2 (en) * 2002-11-06 2009-07-21 Celgene Corporation Methods of using 3-(4-amino-1-oxo-1,3-dihydroisoindol-2-yl)-piperidine-2,6-dione for the treatment and management of myeloproliferative diseases
CL2004001004A1 (en) 2003-05-19 2005-03-18 Upjohn Co PHARMACEUTICAL COMBINATION THAT INCLUDES IRINOTECAN AND REVIMID TO TREAT MULTIPLE MYELOMA.
UA83504C2 (en) 2003-09-04 2008-07-25 Селджин Корпорейшн Polymorphic forms of 3-(4-amino-1-oxo-1,3 dihydro-isoindol-2-yl)-piperidine-2,6-dione
AU2004284075A1 (en) * 2003-10-22 2005-05-06 Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services Pyrrolobenzodiazepine derivatives, compositions comprising the same and methods related thereto
EP1797068B1 (en) 2004-09-03 2013-10-09 Celgene Corporation Processes for the preparation of substituted 2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolines
WO2007136640A2 (en) 2006-05-16 2007-11-29 Celgene Corporation Processes for the preparation of substituted 2-(2,6-dioxopiperidin-3-yl)isoindole-1,3-dione
US20090092343A1 (en) * 2007-10-05 2009-04-09 Mary Thomson Locking Bag with Locking Handle
JP2011513497A (en) * 2008-03-11 2011-04-28 ドクター・レディーズ・ラボラトリーズ・リミテッド Preparation of lenalidomide
WO2009111948A1 (en) 2008-03-13 2009-09-17 天津和美生物技术有限公司 The salts of 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)piperidine-2,6-dione or its derivatives, their polymorphs, preparation methods and uses thereof
US8071638B2 (en) 2008-08-14 2011-12-06 Teva Pharmaceutical Industries Ltd. Solid states of atorvastatin potassium
AU2009321374A1 (en) 2008-11-03 2010-06-03 Generics [Uk] Limited A crystalline form of lenalidomide and a process for its preparation
WO2010054833A1 (en) 2008-11-14 2010-05-20 Ratiopharm Gmbh Intermediate and oral administrative formats containing lenalidomide
AU2009314512B2 (en) 2008-11-17 2013-04-04 Dr. Reddy's Laboratories Ltd. Lenalidomide solvates and processes
DK2403845T3 (en) 2009-03-02 2014-08-04 Generics Uk Ltd Improved process.
WO2010129636A2 (en) 2009-05-08 2010-11-11 Dr. Reddy's Laboratories Ltd. Lenalidomide polymorph
CN101580501B (en) 2009-06-01 2011-03-09 南京卡文迪许生物工程技术有限公司 Synthesis method and intermediate of 3-(substituted dihydroisoindolinone-2-yl)-2,6-piperidinedione
EP2464638A1 (en) 2009-08-12 2012-06-20 Synthon B.V. Lenalidomide salts
WO2011027326A1 (en) 2009-09-03 2011-03-10 Ranbaxy Laboratories Limited Process for the preparation of lenalidomide
WO2011033468A1 (en) 2009-09-16 2011-03-24 Ranbaxy Laboratories Limited Process for the preparation of a crystalline form of lenalidomid
TWI475014B (en) 2009-09-17 2015-03-01 Scinopharm Taiwan Ltd Solid forms of 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2, 6-dione and methods of making the same
WO2011050962A1 (en) 2009-10-29 2011-05-05 Ratiopharm Gmbh Acid addition salts of lenalidomide
CN101696205B (en) 2009-11-02 2011-10-19 南京卡文迪许生物工程技术有限公司 3-(Substituted dihydroisoindol-2-yl)-2,6-piperidinedione polymorph and pharmaceutical composition
WO2011061611A1 (en) 2009-11-19 2011-05-26 Ranbaxy Laboratories Limited Process for the preparation of form b of lenalidomide
WO2011064574A1 (en) 2009-11-24 2011-06-03 Generics [Uk] Limited Hplc method for detecting lenalidomide
WO2011069608A1 (en) 2009-12-09 2011-06-16 Ratiopharm Gmbh S-lenalidomide, polymorphic forms thereof and blend comprising s- und r-lenalidomide
CN101817813B (en) 2010-01-15 2013-04-10 南京卡文迪许生物工程技术有限公司 Crystal IV of 3-(substituted dihydroisoindolinone-2-yl)-2,6-piperidinediketone and medicinal composite thereof
CA2793312C (en) 2010-03-08 2016-06-14 Natco Pharma Limited Anhydrous lenalidomide form-i
CN101791288B (en) 2010-04-07 2011-12-28 南京卡文迪许生物工程技术有限公司 Stable lenalidomide oral solid preparation
CN102453021A (en) * 2010-10-22 2012-05-16 重庆医药工业研究院有限责任公司 Novel crystal form of lenalidomide and preparation method thereof

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6316471B1 (en) * 1996-07-24 2001-11-13 Celgene Corporation Isoindolines, method of use, and pharmaceutical compositions

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
MULLER G.W. ET AL.: 'Amino-substituted thalidomine analogs; potent inhibitors' BIOORGANIC AND MEDICINAL CHEMISTRY LETTERS. vol. 9, 07 June 1999, pages 1625 - 1630, XP004169632 � *

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